EP0461353A1 - Inhibiteurs d'assimilation biogène d'amines - Google Patents

Inhibiteurs d'assimilation biogène d'amines Download PDF

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Publication number
EP0461353A1
EP0461353A1 EP91104766A EP91104766A EP0461353A1 EP 0461353 A1 EP0461353 A1 EP 0461353A1 EP 91104766 A EP91104766 A EP 91104766A EP 91104766 A EP91104766 A EP 91104766A EP 0461353 A1 EP0461353 A1 EP 0461353A1
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Prior art keywords
methyl
benz
methoxy
hexahydro
isoindole
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German (de)
English (en)
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Fatima Z. Basha
John F. De Bernardis
Robert J. Altenbach
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Abbott Laboratories
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Abbott Laboratories
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/26—Psychostimulants, e.g. nicotine, cocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/58—[b]- or [c]-condensed
    • C07D209/62—Naphtho [c] pyrroles; Hydrogenated naphtho [c] pyrroles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/04—Ortho- or peri-condensed ring systems
    • C07D221/06—Ring systems of three rings
    • C07D221/10—Aza-phenanthrenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems

Definitions

  • Disturbances of mood are the most common psychiatric disorders in adults. It has been estimated that 18-23% of women and 8-11 % of men in the United States experience at least one major depressive episode in their lifetimes.
  • no antidepressant drug to date has proven to be superior to electroconvulsive shock therapy in the treatment of severe, suicidal depression.
  • biogenic amine neurotransmitters such as noradrenaline (NA), dopamine (DA) and serotonin (5-HT) in the central nervous system (CNS).
  • NA noradrenaline
  • DA dopamine
  • 5-HT serotonin
  • CNS central nervous system
  • Therapeutic agents can theoretically raise the synaptic levels of these biogenic amine neurotransmitters in the CNS by two principal mechanisms: by inhibition of the neuronal uptake of the biogenic amine neurotransmitters and by inhibition of the metabolic enzymes responsible for converting the biogenic amines to inactive metabolites, such as, for example, monoamine oxidase (MAO).
  • MAO monoamine oxidase
  • Biogenic amine uptake inhibitors including classical antidepressants such as imipramine, desipramine and amitrip- tyline, as well as newer non-classical agents such as fluoxetine (Prozac) are well known to be therapeutically useful in the treatment of affective disorders such as depression, and related CNS disorders.
  • These clinically-effective agents exert their therapeutic effect through the inhibition of the uptake of biogenic amines into neuronal terminals in the CNS, cf: R.W. Fuller, in Antidepressants: Neurochemical, Behavioral and Clinical Perspectives, S.J. Enna, J.D Malick, and E. Richelson, Eds, Raven Press, New York, 1981, pp 1-12; L.E.
  • novel compounds of the present invention are potent inhibitors of biogenic amine neuronal uptake.
  • Other tetrahydrobenz[e]isoindolines and octahydrobenz[h]isoquinolines, which have distinctly different or no known utility, are disclosed by J.F. DeBernardis, et al., U.S. Patent No. 4,618,683, issued October 21, 1986; by J.G. Cannon, et al., J. Med. Chem., 1980, 23:502-505; and by W. Oppolozer, Tetrahedron Letters, 1974, 1001-4.
  • the present invention is directed to compounds that inhibit neuronal biogenic amine uptake of the formula (I): or pharmaceutically-acceptable salts thereof,
  • the present invention is also directed to pharmaceutical compositions comprising a therapeutically-effective amount of a compound of the formula (I) and a pharmaceutically-acceptable carrier or diluent, as well as to a method of treating depression and related affective disorders in humans and lower mammals, by administration of a compound of formula (I).
  • This invention relates to novel compounds of formula (I) which are selective inhibitors of the neuronal uptake of biogenic amines and, therefore, may be used in the treatment of affective disorders, such as, for example, depression.
  • the invention relates to compounds of the formula (I): or pharmaceutically-acceptable salts thereof,
  • m and n are both 0 and R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined above:
  • n is 1 and R 1 , R 2 , R 3, R 4 , R 5 , R 6 and R 7 are as defined above:
  • m is 1, n is 0 and R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined above:
  • C 1 -C 6 -alkoxy refers to a lower alkyl group, as defined below, which is bonded through an oxygen atom.
  • lower alkoxy groups are methoxy, ethoxy, isoprpoxy, t-butoxy, and the like.
  • alkoxyalkyl refers to C 1 -C 6 -alkyl groups, as defined below, which are substituted with an C 1 -C 6 -alkoxy group as defined below.
  • C 1 -C 6 -alkyl refers to branched or straight chain alkyl groups comprising one to six carbon atoms including, but not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl, neopentyl, n-hexyl and the like.
  • C 7 -C 16 -arylalkyl is used herein to mean straight or branched chain radicals of one to six carbon atoms which are substituted with benzene or naphthalene or with a benzoheterocycle, as defined below.
  • benzoheterocycle is used hereinabove to mean a heterocycle to which is fused a benzene ring, such as, for example, 1,3-benzodioxole, 1,4-benzodioxan, indolyl, indolinyl, benzofuryl, benzothienyl, benzimidazolyl; quinolyl, isoquinolyl, dihydroisoquinolyl, tetrahydroisoquinolyl, and the like.
  • Benzoheterocy- cles are attached to the alkyl radical through one of the carbon atoms of the heterocycle.
  • halo-C 1 -C 6 -alkyl refers to a C 1 -C 6 -alkyl group, as defined below, bearing at least one halogen substituent, for example fluoromethyl, chloromethyl, bromomethyl, dichloroethyl, trifluoromethyl, and the like.
  • halogen refers to bromo (Br), chloro (CI), fluoro (F) and iodo (I).
  • heterocycle or “heterocyclic group” as used herein refers to a 5-, 6- or 7-membered ring, wherein one, two or three nitrogen atoms, one sulfur atom, one nitrogen and one sulfur atom, two nitrogen and one sulfur atom, one oxygen atom, or one nitrogen and one oxygen atom replace from one to three of the carbon atoms, and the 5-membered ring has from 0 to 2 double bonds and the 6-membered ring has from 0 to 3 double bonds.
  • Heterocyclic groups include, but are not limited to, N-methylpyrrolyl, pyridyl, pyrimidinyl, furyl, thienyl, N-methylpyrazolyl, oxazolyl, isoxazolyl, 1,2,4-triazolyl, thiadiazolyl, tetrahydrofuryl, N-methylimidazolyl, N-methylpiperazinyl, piperidinyl, pyrrolidinyl, thiazolyl, isoxazolinyl, and the like.
  • Certain compounds of this invention exist in optically active forms.
  • the pure d isomers and pure I isomers, as well as mixtures thereof including the racemic mixtures, are contemplated by this invention. Additional asymmetric centers may be present in a substituent such as an alkyl group. All such isomers as well as mixtures thereof are intended to be within the scope of this invention.
  • stereochemistry of the hydrogen atoms and substituents at the ring junction and at the carbon to which R 2 is attached, as shown in formula (I) can independently be either axial or equatorial unless specifically noted otherwise.
  • reaction schemes IA through VII illustrated below.
  • R I- R 7 as used herein correspond to the R groups identified by formula (I).
  • the reactions are performed in a solvent appropriate to the reagents and materials employed are suitable for the transformation being effected. It is understood by those skilled in the art of organic synthesis that the functionality present on the phenyl ring and other portions of the molecule must be consistent with the chemical transformation proposed. This will, on occasion, necessitate judgment as to the order of synthetic steps, protecting groups required, and deprotection conditions.
  • Substituents on the starting materials may be incompatible with some of the reaction conditions required in some of the methods described, but alternative methods and substituents compatible with the reaction conditions will be readily apparent to skilled practitioners in the art.
  • the use of amino-protecting groups is well known in the art for protecting amino groups against undesirable reactions during a synthetic procedure and many such protecting groups are known, c.f., T.H. Greene, Protective Groups in Organic Synthesis, John Wiley & Sons, New York (1981).
  • the unsaturated nitriles of Formula 2 are prepared by Lewis acid catalyzed trimethylsilyl cyanide addition to known tetralones of Formula 1, followed by acid-catalyzed elimination of the intermediate adduct.
  • the conjugate addition of 2-lithio-2-substituted-1,3-dithianes of the Formula 3 to the unsaturated nitriles of Formula 2 affords the 1,4-Michael addition products of Formula 4 as a mixture of cis and trans isomers.
  • the mercuric chloride catalyzed dithiane-ketal exchange in ethylene glycol/THF at reflux affords the corresponding ketals of Formula 5.
  • the reduction of the nitriles of Formula 5 to the aminomethyl compounds of Formula 6 is accomplished by catalytic hydrogenation with a suitable catalyst such as Raney nickel in a suitable solvent, such as methanol or by treatment with a suitable reducing agent, such as, for example, lithium aluminum hydride.
  • a suitable catalyst such as Raney nickel
  • a suitable solvent such as methanol
  • a suitable reducing agent such as, for example, lithium aluminum hydride.
  • the desired benzoisoindolines of Formula 7 are obtained in a one pot reaction from the hydrolysis of aminomethyl ketals of Formula 6 with a suitable acid, such as hydrochloric acid, in a polar solvent such as THF, to the keto-amine.
  • the keto-amine is in equilibrium with the corresponding iminium compound which is readily reduced by sodium cyanoborohydride.
  • the compounds of Formula 7 are converted to the N-alkylated compounds of Formula IA by alkylation under standard conditions, such as hydrogenation in the presence of a suitable catalyst such as palladium on carbon (Pd/C), and a suitable carbonyl compound, such as, for example, formaldehyde.
  • a suitable catalyst such as palladium on carbon (Pd/C)
  • a suitable carbonyl compound such as, for example, formaldehyde.
  • the 1,4-Michael addition products of Formula 4 are hydrolyzed to the corresponding ketones of Formula 8 with mercuric chloride and a suitable base, such as calcium carbonate, in a suitable polar solvent, such as acetonitrile/water.
  • a suitable polar solvent such as acetonitrile/water.
  • the compounds of Formula 7 are converted to the N-alkylated compounds of Formula IA by alkylation under standard conditions such as hydrogenation in the presence of a suitable catalyst, such as palladium on carbon, and a suitable carbonyl compound such as formaldehyde. Alternately, they may be alkylated by treatment with an alkylating agent, such as dimethyl sulfate or methyl iodide, in the presence of a suitable base, such as sodium hydide, sodium ethoxide or potassium carbonate, in a suitable solvent.
  • a suitable catalyst such as palladium on carbon
  • a suitable carbonyl compound such as formaldehyde
  • an alkylating agent such as dimethyl sulfate or methyl iodide
  • a suitable base such as sodium hydide, sodium ethoxide or potassium carbonate
  • the compounds of Formula 4 are reduced to the aminomethyl dithiane derivatives of Formula 9 with a suitable reducing agent, such as, for example, diborane in THF.
  • a suitable reducing agent such as, for example, diborane in THF.
  • the resulting amino compounds of Formula 9 are acylated with a suitable acylating agent, such as acetic anhydride, in a suitable base such as pyridine, to yield the N-acetyl compounds of Formula 10.
  • N-bromosuccinimide (NBS) catalyzed dithiane hydrolysis of compounds of the Formula 10 in a polar solvent, such as acetone/water or acetonitrile/water, affords the corresponding N-protected keto-amine compounds of Formula 11.
  • N-acetyl group of compounds of Formula 10 Hydrolysis of N-acetyl group of compounds of Formula 10 with a suitable acid such as aqueous hydrochloric acid, followed by intramolecular reductive amination, affords the isoindoline compounds of Formula 7.
  • the compounds of Formula 7 are converted to the N-alkylated compounds of Formula IA by alkylation under standard conditions, such as hydrogenation in the presence of a suitable catalyst, such as palladium on carbon, and a suitable carbonyl compound such as formaldehyde, or by treatment with an alkylating agent, such as dimethyl sulfate or methyl iodide, in the presence of a suitable base, such as sodium hydide, sodium ethoxide or potassium carbonate, in a suitable solvent.
  • a suitable catalyst such as palladium on carbon
  • a suitable carbonyl compound such as formaldehyde
  • an alkylating agent such as dimethyl sulfate or methyl iod
  • the unsaturated nitriles of Formula 2 are converted to the corresponding unsaturated esters by treatment with a suitable acid, such as sulfuric acid, in a suitable alcohol solvent, for example methanol which gives the methyl esters of Formula 12.
  • a suitable acid such as sulfuric acid
  • a suitable alcohol solvent for example methanol which gives the methyl esters of Formula 12.
  • An unsaturated ester of Formula 12 is, in turn, reacted with a nitromethane derivative of Formula 13 to afford an adduct of Formula 14.
  • the adducts of Formula 14 are cyclized to the compounds of Formula 15 by treatment with a suitable reducing agent for reducing the nitro group without reducing the ester, for example zinc and acetic acid.
  • the lactams of Formula 15 are reduced to the isoindoline compounds of Formula 7 with a suitable reducing agent, such as, for example, borane.
  • a suitable reducing agent such as, for example, borane.
  • the compounds of Formula 7 are converted to the N-alkylated compounds of Formula IA by alkylation under standard conditions, such as hydrogenation in the presence of a suitable catalyst, such as palladium on carbon, and a suitable carbonyl compound such as formaldehyde or by treatment with an alkylating agent, such as dimethyl sulfate or methyl iodide, in the presence of a suitable base, such as sodium hydide, sodium ethoxide or potassium carbonate, in a suitable solvent.
  • a suitable catalyst such as palladium on carbon
  • a suitable carbonyl compound such as formaldehyde
  • an alkylating agent such as dimethyl sulfate or methyl iodide
  • the conjugate addition of the compounds of Formula 16 (wherein R 2 may not be substituted with halogen) with the unsaturated nitrile of Formula 2 (wherein R 3 , R 4 , R 5 and R 6 may not be halogen) yields the dinitriles of Formula 17 as a mixture of the cis and trans isomers.
  • Hydrolysis of compounds of Formula 17 with a suitable acid, such as hydrobromic acid in methylene chloride, followed by DMF/water affords the cis imido compounds of Formula 18.
  • Compounds of Formula 18 in which R 2 is hydrogen are alkylated by treatment with a suitable alkylating agent such as methyl iodide or dimethylsulfate in the presence of a suitable base, for example, potasium or sodium t-butoxide or sodium hydride, to afford the compounds of Formula 20.
  • a suitable alkylating agent such as methyl iodide or dimethylsulfate in the presence of a suitable base, for example, potasium or sodium t-butoxide or sodium hydride
  • the compounds of Formula 20 are, in turn, treated sequentially with a Grignard reagent, such as benzyl magnesium bromide, mild acid, for example, hydrochloric acid in methanol, and sodium cyanoborohydride to afford the compounds of Formula IC.
  • an unsaturated nitrile of Formula 2 is condensed with an acetate ester, for example ethyl acetate, in the presence of a suitable base, such as diisopropylamide (LDA), to afford the adducts of Formula 21.
  • a suitable base such as diisopropylamide (LDA)
  • the compounds of Formula 21 are cyclized to the compounds of Formula 22 by reduction of the nitrile group to the aminomethyl group. The reduction can be carried out by catalytic hydrogenation or by treatment with a suitable reducing agent, such as, for example lithium aluminum hydride.
  • the lactams of Formula 22 are alkylated by standard alkylation procedures, for example, treatment with methyl iodide in the presence of a suitable base, such as potassium t-butoxide, to afford the compounds of Formula 23.
  • a suitable base such as potassium t-butoxide
  • the compounds of Formula 23 are treated sequentially with a Grignard reagent, for example, benzylmagnesium chloride, a mild acid, such as methanolic hydrogen chloride, and a suitable reducing agent, preferably sodium cyanoborohydride, to give the isomeric compounds of Formulas IC1, IC2, IC3 and IC4.
  • reaction scheme VA an unsaturated nitrile of Formula 2 is reacted with a ⁇ -keto ester to afford a compound of Formula 24.
  • a compound of Formula 24 is then decarboxylated to afford a keto compound of Formula 25.
  • the ketone of Formula 25 is, in turn, treated with a suitable diol in the presence of a suitable acid catalyst, for example, ethylene glycol in the presence of p-toluenesulfonic acid, to afford a ketal of Formula 26.
  • the compound of Formula 26 is treated with a suitable reducing agent for reducing the cyano group to the amine to afford a compound of Formula 27.
  • the cyano group is preferably reduced by catalytic hydrogenation, for example, over Raney nickel catalyst.
  • An amino compound of Formula 27 is then treated with a suitable reagent for forming separable diastereomeric carbamate derivatives of the amine, for example a compound of Formula 27 is treated with BOC-anhydride to afford the diastereomeric compounds of Formulas 28A (cis) and 28B (trans).
  • the cis diastereomer of a compound of Formula 28 (28A) is treated with a suitable acid, such as trifluoroacetic acid, for simultaneously cleaving the carbamate to afford the free amine and the ketal to form the ketone, which then condense intramolecularly to afford a cyclic imine compound which is, in turn, reduced, preferably with sodium cyanoborohydride, to afford the diastereomeric compounds of Formulas 29 (the cis-anfi isomer) and 31 (the cis-syn isomer).
  • the diastereomeric compounds of Formulas 29 and 31 are separated, for example, by chromatography.
  • the diastereomeric compounds of'Formula 29A and Formula 29B are then treated with a chloroformate derivative of an optically active alcohol, such as, for example menthyl chloroformate (as shown in reaction scheme VB) or alternately, the chloroformate derivative of fenchol., borneol, a-naphthylethanol, myrtanol or nopol, to afford the separable diastereomeric carbamates of Formulas 30A and 30B.
  • a chloroformate derivative of an optically active alcohol such as, for example menthyl chloroformate (as shown in reaction scheme VB) or alternately, the chloroformate derivative of fenchol., borneol, a-naphthylethanol, myrtanol or nopol.
  • the chloroformate derivatives are readily prepared by treating the optically active alcohol with phosgene using standard procedures.
  • the carbamates of Formula 30 are separated and then treated with a suitable reducing agent, for example lithium aluminum hydride, to reduce the carbamate to the N-methyl derivative affording the enantiomeric compounds of Formulas IC2 and IC3.
  • a suitable reducing agent for example lithium aluminum hydride
  • the diastereomeric compounds of Formula 31 are treated in an identical manner to the compounds of Formula 29 to afford the enantiomeric compounds of Formulas IC1 and IC4.
  • the trans diastereomer of a compound of Formula 28 (28B) is treated with a suitable acid, such as trifluoroacetic acid, for simultaneously cleaving the carbamate to afford the free amine and the ketal to form the ketone, which then condense intramolecularly to afford a cyclic imine compound of Formula 33.
  • the imine is, in turn, reduced, preferably with sodium cyanoborohydride, to afford the enantiomeric compounds of Formula 34 (the trans-syn isomer).
  • the compounds of Formula 34 are resolved as described in reaction scheme VB by treatment with a chloroformate derivative of an optically active alcohol to afford the separable diastereomeric carbamates of Formulas 35A1 and 35B1.
  • the carbamates of Formula 30 are separated and then treated with a suitable reducing agent, for example, lithium aluminum hydride, to reduce the carbamate to the N-methyl derivative affording the enantiomeric compounds of Formulas IC5 and IC6.
  • a suitable reducing agent for example, lithium aluminum hydride
  • teralones of Formula 1 are condensed with an acrylate ester, for example, ethyl acrylate, in the presence of pyrrolidine and a suitable acid, such as p-toluenesulfonic acid, to afford the compounds of Formula 36.
  • the compounds of Formula 36 are converted to the compounds of Formula 37 by treatment with a suitable cyano derivative, for example, diethylcyanophosphonate, followed by treatment with a suitable acid, for example p-toluenesulfonic acid in refluxing toluene.
  • the compounds of Formula 37 are cyclized to the lactams of Formula 38 by reduction of the cyano group to the corresponding aminomethyl group which spontaneously condenses with the ester group to form the lactam.
  • the lactams of Formula 38 are converted to the compounds of Formula VI as described in reaction scheme IV for the conversion of the compounds of Formula 22 to the compounds of Formula ID.
  • a racemic compound of Formula 38 is treated with a suitable base, such as, for example potassium t-butoxide, and benzyl bromide to give the N-protected compound, which is, in turn, treated with a Grignard reagent, as described previously in reaction scheme IV for the conversion of the compounds of Formula 22 to the compound of Formula IV, to afford a racemic compound of Formula VI.
  • a racemic compound of Formula VI is then condensed with (-) menthyl chloroformate to afford the diastereomeric carbamates of Formulas 40A and 40B.
  • the compounds of Formula 29 and 30 are treated with a suitable reducing agent, such as, for example, lithium aluminum hydride to afford the optically active compounds of Formulas ID1 and ID2.
  • salts which are, within the scope of sound medical judgement, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio, effective for their intended use in the treatment of depression and related mood and effective disorders.
  • the salts can be prepared in situ during the final isolation and purification of the compounds of Formula (I), or separately by reacting the free base function with a suitable acid or cation.
  • Representative acid addition salts include hydrochloride, hydrobromide, sulfate, bisulfate, acetate, oxalate, valerate, oleate, palmitate, stearate, laurate, borate, benzoate, lactate, phosphate, toluenesulfonate, methanesulfonate, citrate, maleate, fumarate, succinate, tartrate, ascorbate, glucoheptonate, lactobionate, lauryl sulfate salts and the like.
  • Representative alkali or alkaline earth metal salts include sodium, calcium, potassium, magnesium salts and the like.
  • cognate disorder refers to disorders that are characterized by changes in mood as the primary clinical manifestation, cf, R.J. Baldessarini in Goodman and Gilman's The Pharmacological Basis of Therapeutics, A.G. Gilman, L.S. Goodman, T.W. Rail and F. Murad, Eds., Macmillan, New York, i g 8-5,-pF412-432.
  • biogenic amine uptake refers to the selective, systems for attenuating and terminating the affects of the biogenic amines by actively transporting them into nerve terminals and subsequently, into storage granules.
  • depression refers to "major depression” as defined in the seventh edition of Goodman and Gilman's "The Pharmacological Basis of Therapeutics". Major depression is distinguishable from normal grief, sadness and disappointment and is characterized by feelings of intense sadness and despair, mental slowing and loss of concentration, pessimistic worry, agitation and self-deprecation. Physical changes also occur, including insomnia, anorexia and weight loss, decreased energy and libido, and disruption of hormonal circadian rhythms.
  • the compounds of formula (I) inhibit the uptake of biogenic amine neurotransmitters into nerve terminals and, therefore, are useful in treatment of affective disorders.
  • diseases include major depression and the dipolar disorder, manic-depressive illness.
  • the compounds of this invention may also be useful in the treatment of depression associated with other forms of mental illness, such as, for example, psychosis and dementia.
  • ligand-carrier binding assays were carried out as an initial sceen.
  • the ability of the compounds of the invention to interact with biogenic amine uptake carriers and to inhibit the neuronal uptake of biogenic amines can be demonstrated in vitro using the following protocols.
  • the hypothalamus which was used for norepinephrine uptake studies, was removed from the posterior part by using the anterior commissure as the horizontal reference point and a line between the posterior hypothalamus and mammillary bodies as the caudal limit.
  • the striatum which was used for dopamine uptake studies, was also dissected from the posterior portion using the external wall of the lateral ventricle as the internal limit and the corpus collosum as the external limit.
  • the frontal parts of the striatum were removed from the anterior portion of the cerebrum and combined with the striatal tissue from the posterior segment.
  • the cortex which was used for serotonin uptake studies, was composed of the rest of the anterior portion of the cerebrum and the cortical surfaces removed from the posterior segment.
  • hypothalamus and the striatum each weighed about 100 mg or slightly less, whereas the cortex weighed up to 800 mg.
  • the tissues were placed in a cold Potter-Elvehjem glass homogenizer with 5 (cortex) or 10 (hypothalamus) or 20 (striatum) volumes of ice-cold 0.32 M sucrose, pH 7, and homogenized by hand.
  • the homogenate was centrifuged (on a Multifugeo, American Scientific Products) at 2500 rpm for 10 minutes in a refrigerated room (- 4 0 C).
  • the supernatant fraction containing the synaptosomes was decanted, mixed thoroughly and kept on crushed ice for use in the uptake studies.
  • the modified Krebs-Ringer bicarbonate buffer used in these studies contained 118 mM sodium chloride, 4 mM potassium chloride, 1.3 mM calcium chloride, 1.12 mM potassium dihydrogen phosphate, 1.2 mM magnesium sulfate and 24 mM sodium bicarbonate, with the addition of 5 mM glucose, 0.15 mM disodium EDTA, 12.5 ⁇ M nialamide and 1 mM ascorbic acid. Uptake was initiated by the addition of the tritiated amine and the mixture was incubated at 37 0 C in a Dubnoff Metabolic Shaking Incubator for 4 minutes.
  • the term "pharmaceutically acceptable carrier” means a non-toxic, inert solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type.
  • materials that can serve as pharmaceutically acceptable carriers are sugars, such as lactose, glucose and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as propylene glycol; polyols such as glycerin, sorbitol, mannitol and polyethylene glycol; esters such as ethyl oleate and ethyl laur
  • wetting agents such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, and preservatives can also be present in the composition, according to the judgement of the formulator.
  • the compounds of the present invention may be administered alone or in combination or in concurrent therapy with other agents.
  • the specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed; and like factors well known in the medical arts.
  • the total daily dose of the compounds of this invention administered to a host in single or in divided doses can be in amounts, for example, from 0.01 to 25 mg/kg body weight or more usually from 0.1 to 15 mg/kg body weight.
  • Single dose compositions may contain such amounts or submultiples thereof to make up the daily dose.
  • treatment regimens according to the present invention comprise administration to a patient in need of such treatment from about 10 mg to about 1000 mg of the compound(s) of this invention per day in multiple doses or in a single dose of from 10 mg to 1000 mg.
  • compositions in unit dosage forms comprising a therapeutically effective amount of a compound (or compounds) of this invention in combination with a conventional pharmaceutical carrier.
  • sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol.
  • acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S.P. and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil can be employed including synthetic mono- or diglycerides.
  • fatty acids such as oleic acid are used in the preparation of injectables.
  • the most common way to accomplish this is to inject a suspension of crystalline or amorphous material with poor water solubility.
  • the rate of absorption of the drug becomes dependent on the rate of dissolution of the drug which is, in turn, dependent on the physical state of the drug, for example, the crystal size and the crystalline form.
  • Another approach to delaying absorption of a drug is to administer the drug as a solution or suspension in oil.
  • Injectable depot forms can also be made by forming microcapsule matrices of drugs and biodegradable polymers such as polylactide-polyglycolide.
  • the rate of drug release can be controlled.
  • biodegradable polymers include poly-orthoesters and polyanhydrides. Depot injectables can also be made by entrapping the drug in liposomes or microemulsions which are compatible with body tissues.
  • Suppositories for rectal administration of the drug can be prepared by mixing the drug with a suitable nonirritating excipient such as cocoa butter and polyethylene glycol which are solid at ordinary temperature but liquid at the rectal temperature and will therefore melt in the rectum and release the drug.
  • a suitable nonirritating excipient such as cocoa butter and polyethylene glycol which are solid at ordinary temperature but liquid at the rectal temperature and will therefore melt in the rectum and release the drug.
  • Solid dosage forms for oral administration may include capsules, tablets, pills, powders, prills and granules.
  • the active compound may be admixed with at least one inert diluent such as sucrose, lactose or starch.
  • Such dosage forms may also comprise, as is normal practice, additional substances other than inert diluents, e.g., tableting lubricants and other tableting aids such as magnesium stearate and microcrystalline cellulose.
  • the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings and other release-controlling coatings.
  • Liquid dosage forms for oral administration may include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs containing inert diluents commonly used in the art such as water.
  • Such compositions may also comprise adjuvants, such as wetting agents; emulsifying and suspending agents; sweetening, flavoring and perfuming agents.
  • the compounds of the present invention can be incorporated into slow release or targeted delivery systems such as polymer matrices, liposomes and microspheres. They may be sterilized, for example, by filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can dissolve in sterile water, or some other sterile injectable medium immediately before use.
  • the active compounds can also be in micro-encapsulated form with one or more excipients as noted above.
  • Dosage forms for topical or transdermal administration of a compound of this invention further include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches.
  • the active component is admixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required.
  • Ophthalmic formulations, ear drops, eye ointments, powders and solutions are also contemplated as being within the scope of this invention.
  • the ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.
  • excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.
  • Powders and sprays can contain, in addition to the compounds of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances.
  • Sprays can additionally contain customary propellants such as chlorofluorohydrocarbons.
  • Transdermal patches have the added advantage of providing controlled delivery of a compound to the body.
  • dosage forms can be made by dissolving or dispersing the compound in the proper medium.
  • Absorption enhancers can also be used to increase the flux of the compound across the skin.
  • the rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel.
  • Trimethylsilylcyanide (50.0 g, 510 mmol) was added to a suspension of 75.0 g (430 mmol) of 6-methoxy-a-tetralone (commercially available from Aldrich Chemical Company) in 75 mL of anhydrous tetrahydrofuran (THF) at ambient temperature.
  • Lithium cyanide 100 mL of a 0.5 M solution in N,N-dimethylformamide (DMF) was added to the resultant mixture in one portion.
  • the reaction mixture was stirred at ambient temperature for 1.5 h and then the THF was removed under reduced pressure.
  • the concentrate was partitioned between diethyl ether and water (5:1 v/v).
  • the aqueous layer was extracted with diethyl ether and the combined organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure.
  • the residue was dissolved in 400 mL of anhydrous toluene, containing 15 g of p-toluenesulfonic acid, previously refluxed in order to remove residual water by azeotropic distillation. The mixture was heated at reflux (with a Dean Stark trap) for 1 h.
  • the resultant solution was cooled to ambient temperature and washed with cold 1 N aqueous sodium hydroxide solution.
  • the organic layer was separated, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo.
  • Step 4 1-Cyano-6-methoxy-2-[1-(1,3-dioxolane)-2-phenylethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 5 1-Aminomethyl-6-methoxy-2-[1-(1,3-dioxolane)-2-phenylethyl]-1,2,3,4-tetrahydronaphthalene
  • the residue was adsorbed onto silica gel and purified on silica gel eluted with ethyl acetate:formic acid:water (8:1:1, v/v/v) to give the formic acid salt of the desired product which was dissolved in water.
  • the aqueous solution was made basic by the addition of sodium hydroxide and then extracted with methylene chloride.
  • the title compound was purified by conversion to the corresponding hydrochloride salt by treatment of the residue from the hydrogenation reaction with methanol saturated with anhydrous hydrogen chloride.
  • the hydrochloride salt of the title compound was recrystallized from diethyl ether/ethyl alcohol to afford the hydrochloride salt of the title compound in 78% yield.
  • Step 6 cis/trans 2,3,3a,4,5,9b-Hexahydro-7-methoxy-3-phenylmethyl-1H-benz[e]isoindolehydrochloride
  • the free amine was prepared by dissolving the formic acid salt in water, adding sodium hydroxide to make the solution basic and extracting the basic solution with methylene chloride. The methylene chloride was removed under reduced pressure and the residue was dissolved in diethyl ether saturated with anhydrous hydrogen chloride. The desired hydrochloride salt was collected by filtration, m.p.
  • the aqueous layer was extracted twice with ethyl acetate and the combined organic layers were washed with dilute aqueous sodium hydroxide solution, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo.
  • the residue was dissolved in 20 mL of anhydrous THF and borane-THF complex (15 mL of a 1.0 M solution in THF, 15 mmol) was added to the resultant solution.
  • the reaction mixture was heated at reflux for 1 h.
  • the THF was removed in vacuo and the residue was dissolved in 20 mL of methanol saturated with anhydrous hydrogen chloride.
  • the solution was heated at reflux overnight and the solvent was removed in vacuo.
  • the mixture was transferred to a separatory funnel and 1 N aqueous hydrochloric acid solution and 4 mL of methylene chloride were added. The layers were separated and the aqueous layer was extracted with two portions of methylene chloride. The combined organic layers were washed with 1 N aqueous hydrochloric acid solution and 1 N dilute aqueous sodium hydroxide solution, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo.
  • the reaction mixture was then filtered and the filtrate was concentrated in vacuo.
  • the solid residue was dissolved in ethyl acetate and the ethyl acetate solution was washed with 1 N aqueous hydrochloric acid solution and 1 N aqueous sodium hydroxide solution, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo.
  • the residue was dissolved in 20 mL of anhydrous THF and borane (3.5 mL of a 1.0 M solution in THF, 3.5 mmol) was added to the resultant solution.
  • the reaction mixture was heated at reflux under a nitrogen atmosphere for 2 h.
  • Step 3 1-Cyano-2-[1-(1,3-dioxolane)-2-phenylethyl-1,2,3,4-tetrahydronaphthalene
  • Step 4 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-phenylethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 6 cis-2,3,3a,4,5,9b-Hexahydro-2-methyl-3-phenylmethyl-1H-benz[e]isoindole methanesulfonic acid salt
  • Step 3 1-Cyano-2-[1-(1,3-dioxolane)-2-(3-methylphenyl)ethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 4 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-(3-methylphenyl)ethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 5 cis-2,3,3a,4,5,9b-Hexahydro-3-(3-methylphenyl)methyl-1H-benz[e]isoindolehydrochloride
  • Step 3 trans-2,3,3a,4,5,9b-Hexahydro-2-methyl-3-(3-methylphenyl)methyl-1 H-benz[e]isoindole methanesulfonic acid salt
  • 1,3-Dithiane (12 g, 0.1 mol) was dissolved in 150 mL of anhydrous THF under a nitrogen atmosphere.
  • the resultant solution was cooled to -78° C and n-butyllithium (44 mL of a 2.5 M solution of in hexane, 0.11 mol) was added.
  • the reaction mixture was warmed to -23 °C and then stirred at 23° C for 0.5 h.
  • the reaction mixture was recooled to -78° C and 25 g (0.135 mol) of 3-fluorobenzyl bromide was added over a 15 minute period.
  • Step 3 1-Cyano-2-[1-(1,3-dioxolane)-2-(3-fluorophenyl)ethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 4 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-(3-fluorophenyl)ethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 5 cis-3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1 H-benz[e]isoindole hydrochloride
  • 1,3-Dithiane (20 g, 166 mmol) was dissolved in 250 mL of anhydrous THF under a nitrogen atmosphere.
  • the resultant solution was cooled to -78° C and n-butyllithium (128 mL of a 1.5 M solution of in hexane, 199 m mol) was added.
  • the reaction mixture was warmed to 0°C and then stirred at 0°C for 0.5 h.
  • the reaction mixture was recooled to -78° C and 25 g (0.135 mol) of 3-fluorobenzyl bromide was added over a 15 minute period.
  • the reaction mixture was stirred for 3 h at ambient temperature and then the reaction was quenched with aqueous ammonium chloride solution.
  • reaction mixture was allowed to warm to ambient temperature, stirred at ambient temperature for 2 h and then the reaction was quenched with concentrated aqueous ammonium chloride solution.
  • the resultant layers were separated and the aqueous layer was extracted with two portions of ethyl acetate.
  • the combined organic extracts were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo.
  • Step 3 1-Cyano-2-[1-(1,3-dioxolane)-2-(4-fluorophenyl)ethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 4 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-(4-fluorophenyl)ethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 5 3-(4-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1H-benz[e]isoindole methanesulfonic acid salt
  • Step 2 1-Cyano-2-[1-(13-dithiane)-2-(3-methoxyphenyl)ethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 3 1-Cyano-2-[1-(1,3-dioxolane)-2-phenylethyl]-5-methoxy-1,2,3,4-tetrahydronaphthalene
  • the oil was separated and partitioned between methylene chloride and water (4:1 v/v).
  • the organic layer was saved and the aqueous layer was extracted with methylene chloride.
  • the purple material was also partitioned between methylene chloride and water (4:1 v/v) .
  • the organic layer was again saved and the aqueous layer was extracted with two portions of methylene chloride. All of the organic layers were then combined, washed with two portions of water and then adsorbed onto silica gel.
  • Step 4 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-phenylethyl]-5-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 5 cis-2,3,3a,4,5,9b-Hexahydro-6-methoxy-3-phenylmethyl-1 H-benz[e]isoindole methanesulfonic acid salt
  • the residue was partitioned between 15% aqueous potassium hydroxide solution and methylene chloride (1:5 v/v) and the aqueous layer was extracted with two portions of methylene chloride.
  • the combined organic layers were concentrated in vacuo.
  • the residue was treated with methanol saturated with anhydrous hydrogen chloride and the solution was concentrated in vacuo.
  • the residue was dried with toluene three times and then dissolved in hot acetone.
  • the crystals which precipitated upon cooling to ambient temperature were dissolved in aqueous potassium hydroxide solution and the aqueous solution was extracted with four portions of methylene chloride.
  • the combined organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo.
  • Step 1 1-Cyano-2-[1-(1,3-dithiane)-2-(3-fluorophenyl)ethyl]-5-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 2 1-Cyano-2-[1-(1,3-dioxolane)-2-(3-fluorophenyl)ethyl]-5-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 3 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-(3-fluorophenyl)ethyl]-5-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 4 3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-6-methoxy-1H-benz[e]isoindole
  • Step 5 cis-3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-6-methoxy-2-methyl-1 H-benz[e]isoindole hydrochloride
  • Step 1 1-Cyano-2-[1-(13-dithiane)-2-(3-fluorophenyl)ethyl]-6-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 1 1-Cyano-2-[1-(1,3-dioxolane)-2-(3-fluorophenyl)ethyl]-6-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 2 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-(3-fluorophenyl)ethyl]-6-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 3 cis-3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-7-methoxy-1H-benz[e]isoindole
  • Step 4 cis-3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-7-methoxy-2-methyl-1H-benz[e]isoindole hydrochloride
  • Step 1 1-Cyano-2-[1-(1,3-dithiane)-2-(3-methoxyphenyl)ethyl]-6-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 2 1-Cyano-2-[1-(1,3-dioxolane)-2-(3-methoxyphenylethyl]-6-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 3 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-(3-methoxyphenyl)ethyl]-6-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 5 cis-2,3,3a,4,5,9b-Hexahydro-7-methoxy-3-(3-methoxyphenyl)methyl-2-methyl-1H-benz[e]isoindole methanesulfonic acid
  • Step 3 1-Cyano-2-[1-(1,3-dioxolane)-4-phenylbutyl]-6-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 4 1-Aminomethyl-2-[1-(1,3-dioxolane)-4-phenylbutyl]-6-methoxy-1,2,3,4-tetrahydronaphthalene
  • the residue was dissolved in 40 mL of methanol and 1 g of sodium cyanoborohydride was added to the resultant solution followed by a few crystals of bromocresol green indicator.
  • the pH of the solution was adjusted with methanolic hydrogen chloride until the color of the solution changed from yellow to greenish blue.
  • the solvent was removed in vacuo and the residue was dissolved in 2 N aqueous hydrochloric acid in order to quench any excess sodium cyanoborohydride and the resultant aqueous solution was extracted with diethyl ether. The aqueous layer from the ether extraction was then extracted with methylene chloride.
  • Step 6 cis-2,3,3a,4,5,9b-Hexahydro-7-methoxy-2-methyl-3-(3-phenylpropyl)-1H-benz[e]isoindole methanesulfonic acid salt
  • Step 1 1-Cyano-5,6-dimethoxy-2-[1-(1,3-dithiane)-2-phenylethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 2 1-Cyano-5,6-dimethoxy-2-[1-(1,3-dioxolane)-2-phenylethyl-1,2,3,4-tetrahydronaphthalene
  • Step 3 1-Aminomethyl-5,6-dimethoxy-2-[1-(1,3-dioxolane)-2-phenylethyl]-1,2;3,4-tetrahydronaphthalene
  • Step 4 cis-6,7-Dimethoxy-2,3,3a,4,5,9b-hexahydro-3-phenylmethyl-1H-benz[e]isoindole hydrochloride
  • Step 3 trans-6,7-Dimethoxy-2,3,3a,4,5,9b-hexahydro-3-(3-methylphenyl)methyl-1H-benz[e]isoindole methanesulfonic acid salt
  • Example 7 Following the procedures described in Example 7, replacing the product of Example 6 with 1.17 g (3.62 mmol) of the product of Example 33, the desired product was prepared and converted to the hydrochloride salt (the title compound), m.p.100-104°C; MS DCl-NH 3 M/Z: 352 (M+H) +. Analysis calculated for C 23 H 30 ClNO 2 +H 2 O: C, 68.05; H, 7.95; N, 3.45. Found: C, 64.47; H, 7.57; N, 3.34.
  • Step 4 trans-2,3,3a,4,5,9b-Hexahydro-2-methyl-6,7-methylenedioxy-3-(3-methylphenyl)methyl-1H-benz[e]-isoindole methanesulfonic acid salt
  • Example 2 Following the procedures described in Example 2, replacing the product of Example 1 with 2.27 g (7.07 mmol) of 2,3,3a,4,5,9b-hexahydro-6,7-methylenedioxy-3-(3-methylphenyl)methyl-1 H-benz[e]isoindole from Step 3 of this Example, the title compound was prepared, m.p.
  • Step 3 3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-6,7-methylenedioxy-1H-benz[e]isoindole methanesulfonic acid salt
  • Step 4 trans 3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-2-methyl-6,7-methylenedioxy-1 H-benz[e]-isoindole methanesulfonic acid salt
  • Example 2 Following the procedures described in Example 2, replacing the product of Example 1 with 3-(3-fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-6,7-methylenedioxy-1H-benz[e]isoindole from Step 3 of this Example, the title compound was prepared, m.p.
  • Step 3 1-Cyano-2-[1-(1,3-dioxolane)-2-phenylethyl]-5-methoxy-8-methyl-1,2,3,4-tetrahydronaphthalene
  • Step 4 1-Aminomethyl-2-[1-(1,3-dioxolane)-2-phenylethyl]-5-methoxy-8-methyl-1,2,3,4-tetrahydronaphthalene
  • Step 5 cis-2,3,3a,4,5,9b-Hexahydro-6-methoxy-9-methyl-3-phenylmethyl-1 H-benz[e]isoindole hydrochloride
  • Step 1 1-Cyano-2-[1-(1,3-dithiane)-2-phenylethyl]-8-(4-(4-fluorophenyl)-1-n-butoxy)-5-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 2 1-Cyano-2-[1-(1,3-dioxolane)-2-phenylethyl]-8-(4-(4-fluorophenyl)-1-n-butoxy)-5-methoxy-1,2,3,4-tetrahydronaphthalene
  • Step 3 1-Aminomethyl-2-[1 -(1,3-dioxolane)-2-phenylethyl]-8-(4-(4-fluorophenyl)-1-n-butoxy)-5-methoxy-1,2,3,4-tetrahydronaphthatene
  • Step 4 9-(4-(4-Fluorophenyl)-1-n-butoxy)-2,3,3a,4,5,9b-hexahydro-6-methoxy-3-phenylmethyl-1H-benz[e]-isoindole hydrochloride
  • Step 5 cis-2-Ethyl-9-(4-(4-fluorophenyl)butyloxy)-2,3,3a,4,5,9b-hexahydro-6-methoxy-3-phenylmethyl-1H-benz[e]isoindole methanesulfonic acid salt
  • Example 4 Following the procedures described in Example 3, replacing the product of Example 1 with 0.90 g (2.0 mmol) of 9-(4-(4-fluorophenyl)-1-n-butoxy)-2,3,3a,4,5,9b-hexahydro-6-methoxy-3-phenylmethyl-1 H-benz[e]-isoindole hydrochloride, from Step 4, the title compound was prepared as white needle-like crystals, m.p.
  • Step 1 1-Cyano-2-[1-(13-dithiane)-2-(3-fluorophenyl)ethyl]-5,6,7-trimethoxy-1,2,3,4-tetrahydronaphthalene
  • Step 3 trans-3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-6,7,8-trimethoxy-1H-benz[e]isoindole
  • Step 4 trans-3-(3-Fluorophenyl)-methyl-2,3,3a,4,5,9b-hexahydro-2-methyl-6,7,8-trimethoxy-1H-benz[e]-isoindole hydrochloride
  • Step 1 1-Cyano-2-[1-(13-dithiane)-2-(3-fluorophenyl)ethyl]-5,6,8-trimethoxy-1,2,3,4-tetrahydronaphthalene
  • Step 3 3-(3-Fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-6,7,9-trimethoxy-1 H-benz[e]isoindole hydrochloride
  • Step 4 3-(3-Fluorophenyl)-methyl-2,3,3a,4,5,9b-hexahydro-2-methyl-6,7 9-trimethoxy-1 H-benz[e]isoindole hydrochloride:
  • the title compound was prepared by the procedures described in Step 2 of Example 1, replacing 6-methoxy-a-tetralone with 5,6-dimethoxy-8-fluoro-a-tetralone (prepared as described by J.F. DeBernardis et al. in Example Numbers 62 - 67 in U.S. Patent Number 4,634,705, issued January 6, 1987).
  • Step 2 1-Cyano-5,6-dimethoxy-2-[1-(1,3-dithiane)-2-(3-fluorophenyl)ethyl]-8-fluoro-1,2,3,4-tetrahydronaphthalene:
  • Step 3 1-Cyano-5,6-dimethoxy-8-fluoro-2-(3-fluorophenyl)methylcarbonyl-1,2,3,4-tetrahydronaphthalene:
  • Step 4 6,7-Dimethoxy-9-fluoro-3-(3-fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1H-benz[e]isoindole
  • Step 5 6,7,-Dimethoxy-9-fluoro-3-(3-fluorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-2-methyl-1H-benz[e]-isoindole hydrochloride
  • Step 1 7-Bromo-1-cyano-2-[1-(1,3-dithiane)-2-phenylethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 2 1-Aminomethyl-6-bromo-2-[1-(1,3-dithiane)-2-phenylethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 3 1-(N-Acetyl)aminomethyl-6-bromo-2-[1-(1,3-dithiane)-2-phenylethyl]-1,2,3,4-tetrahydronaphthalene
  • Step 4 1-(N-Acetyl)aminomethyl-6-bromo-2-phenylmethylcarbonyl-1,2,3,4-tetrahydronaphthalene
  • N-Bromosuccinimide (NBS; 16.6 g (93.5 mmol) was dissolved in 500 mL of 97:3 acetone :water and the resultant mixture was cooled to 0°C.
  • 1-(N-acetyl)aminomethyl-6-bromo-2-[i-(1,3-dithiane)-2-phenylethyl]-1,2,3,4-tetrahydronaphthalene (5.73 g, 11.68 mmol) from Step 3 was dissolved in 100 mL of 97:3 acetone:water and the resultant solution was added to the NBS solution over a 10 min period.
  • Step 5 cis-7-Bromo-2,3,3a,4,5,9b-hexahydro-3-phenylmethyl-1H-benz[e]isoindole methanesulfonic acid salt
  • the residue was dissolved in water and the solution was made basic by the addition of concentrated aqueous sodium hydroxide solution.
  • the aqueous solution was extracted with three portions of methylene chloride and the combined organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo.
  • the concentrated solution was adsorbed onto silica gel.
  • the dried silica gel was loaded onto a silica gel column and eluted with ethyl acetate:formic acid:water (18:1:1) to give 1.7 g (40% yield) of the formic acid salt of the desired product.
  • the formic acid salt was converted to the methanesulfonic acid salt via the free amine to give the title compound, m.p.
  • reaction mixture was then allowed to cool to ambient temperature and was stirred at ambient temperature for approximately 64 h.
  • the solvents were removed in vacuo and the residue was made basic by the addition of 1 N aqueous sodium hydroxide solution and the resultant aqueous mixture was extracted with three portions of methylene chloride The combined organic extract was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo.
  • Step 3 1-(1-Carbomethoxy-1,2,3,4-tetrahydro-2-naphthyl)-2-(3-nitrophenyl)-1-nitroethane
  • Step 4 3-(3-Acetaminophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1 H-oxo-benz[e]isoindoie
  • Step 5 3-(5-Acetamino-2-chlorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1 H-oxo-benz[e]isoindole
  • Step 6 3-(5-(N-Ethyl)amino-2-chlorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1 H-oxo-benz[e]isoindole
  • Step 7 cis-3-(3-Chloro-4-N-ethyl-N-methylaminophenyl)methyl-2,3,3a,4,5,9b-hexahydro-2-methyl-1H-benz-[e]isoindole hydrochloride
  • Step 4 1- (1-Carbomethoxy-1,2,3,4-tetrahydro-2-naphthyl)-2-(3-chlorophenyl)-1-nitroethane
  • Step 5 3-(3-Chlorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1 H-oxo-benz[e]isoindole
  • 6-Chloro-1-cyano-3,4-dihydronaphthalene (5 g, 263 mmol), lit ref, was dissolved in 77% sulfuric acid in methanol and the resulting solution was heated at 95-100° C for 2.5 h. The reaction mixture was allowed to cool to ambient temperature and 45 mL was added, followed by 5 mL of water. The reaction mixture was stirred at ambient temperature for 2 days and then concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic layer was concentrated in vacuo.
  • Step 2 1-(1-Carbomethoxy-6-chloro-1,2,3,4-tetrahydro-2-naphthyl)-2-(3-chlorophenyl)-1-nitroethane
  • Step 3 7-Chloro-3-(3-chlorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1H-oxo-benz[e]isoindole
  • Step 4 7-Chloro-3-(3-chlorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1H-benz[e]isoindole
  • Example 48 Following the procedures described in Example 44, replacing 7-bromo-2,3,3a,4,5,9b-hexahydro-3-phenylmethyl-1H-benz[e]isoindole with 1.35 g (4.05 mmol) 7-chloro-3-(3-chlorophenyl)methyl-2,3,3a,4,5,9b-hexahydro-1 H-benz[e]isoindole, from Step 4, the title compound was prepared as a mixture with Example 49. The two diastereomers were separated by chromatography on silica gel eluted with 2:1 diethyl ether: hexane saturated with ammonium hydroxide. Example 48 was obtained in 40% yield (0.56 g), m.p.
  • Step 1 1-Cyano-2-(1-cyano-2-phenyl-1-ethyl)-1,2,3,4-tetrahydronaphthalene
  • reaction mixture was stirred for 45 min at -78° C and then a solution of 3.1 g (20 mmol) of 1-cyano-3,4-dihydronaphthalene (the product of Step 1 of Example 9) in 40 mL of THF was added.
  • the reaction mixture was stirred at -78 C for 0.5 h and then the reaction was quenched by pouring the reaction mixture into saturated aqueous ammonium chloride solution. The layers were separated and the aqueous layer was extracted with ethyl acetate.
  • Step 3 1,2,3,4,4a,5,6,10b-Octahydro-4-phenylmethyl-benz[f]isoquinoline methanesulfonic acid salt
  • Example 50 The product of Example 50 was subjected to reductive methylation as described in Example 2. The two diastereomers of the desired product were separated by chromatography on silica gel eluted with 2:1 diethyl ether:hexane saturated with ammonium hydroxide to give the title compound and 52 as the free amine products.
  • Step 3 8-Methoxy-1,2,3,4,4a,5,6,10b-octahydro-benz[f]isoquinoline methanesulfonic acid salt
  • Example 53 The product of Example 53 was subjected to reductive methylation as described in Example 2. The two diastereomers of the desired product (formed in a ratio of 10:1 cis:trans) were not separated by chromatography. The free amine of the title compound was obtained in 84% yield (670 mg) and converted to the hydrochloride salt, m.p 107-114° C; MS DCl-NH 3 M/Z: 232 (M+H) + 1 H NMR (CDCl 3 ) ⁇ 1.09 (3H, t), 1.47-1.55 (1 H, m), 1.61-1.76 (2H, m), 1.97-2.17 (4H, m), 2.34-2.48 (2H, m), 2.67-2.84 (4H, m), 2.87 (3H, s), 2.97-3.06 (1H, m), 3.77 (3H, s), 6.61 (1H, d), 6.71 (1H, dd), 7.06 (1H, d). Analysis calculated for C 16 H 25 NO 4 S+0.2
  • Step 1 1-Cyano-2-(1-cyano-2-phenyl-1-ethyl)-1,2,3,4-tetrahydronaphthalene
  • Step 2 1,3-Dioxo-8-methoxy-1,2,3,4,4a,5,6,10b-octahydro-4-phenylmethyl-benz[f]isoquinoline
  • Step 4 2-Ethyl-8-methoxy-1,2,3,4,4a,5,6,10b-octahydro-4-phenylmethyl-benz[f]isoquinoline methanesulfonic acid salt
  • Step 1 1,3-Dioxo-8-hydroxy-1,2,3,4,4a,5,6,10b-octahydro-4-phenylmethyl-benz[f]isoquinoline
  • reaction mixture was poured onto ice and the aqueous mixture was made basic by the addition of solid sodium carbonate, followed by saturated aqueous sodium bicarbonate solution and then 45% aqueous sodium hydroxide solution. The mixture was kept cold ( ⁇ 0° C) during the pH adjustment. The aqueous mixture was extracted with three portions of methylene chloride. The combined organic extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure.
  • Step 2 1,3-Dioxo-8-ethoxy-2-ethyl-1,2,3,4,4a,5,6,10b-octahydro-4-phenylmethyl-benz[f]isoquinoline
  • Step 3 2,10b-Diethyl-8-ethoxy-1,2,3,4,4a,5,6,10b-octahydro-4-phenylmethyl-benz[f]isoquinoline methanesulfonic acid salt
  • Examples 58 - 70 are prepared as disclosed in Table 1.
  • n-Butyl lithium (14.2 mL of a 2.5 M solution in hexane, 35.4 mmol) was added to a solution of diisopropylamine (6.77 mL, 48 mmol) in 100 mL of dry THF at -78° C under a nitrogen atmosphere. The solution was stirred at - 78° C for 15 min and then ethyl acetate (3.3 mL , 33.8 mmol) was added dropwise over a 10 min period. The solution was stirred at -78° C for 30 min.
  • Step 2 cis-1,2,3,4,4a,5,6,10b-Octahydro-3-oxo-benz[f]isoquinoline
  • Step 3 cis-2-Methyl-1,2,3,4,4a,5,6,10b-octahydro-3-oxo-benz[f]isoquinoline
  • Step 4 cis-2-Methyl-1,2,3,4,4a,5,6,10b-octahydro-3-phenylmethyl-benz[f]isoquinoline
  • Step 1 cis-8-Methoxy-1,3-dioxo-2-methyl-1,2,3,4,4a,5,6,10b-octahydro-benz[f]isoquinoline
  • n-Butyl lithium (8.1 mL, 20.196) was added to a solution of 3.9 mL (27.54 mmol) of diisopropylamine in 25 mL of THF at -78 C.
  • a solution of acetonitrile (1.01 mL, 18.54 mmol) in 10 mL of dry THF was then added dropwise. The resultant solution was stirred at -78 C for 1 h.
  • the residue was redissolved in methylene chloride and adsorbed onto silica gel and chromatographed on silica gel eluted with hexane/ethyl acetate (7:1) to give the intermediate acetonitrile adduct.
  • the intermediate was dissolved in 100 mL of methylene chloride and hydrogen bromide gas was bubbled into the solution at 0° C for 1 h.
  • the methylene chloride was evaporated at ambient temperature with a stream of nitrogen gas.
  • the residue was added to 50 mL of a 1:1 mixture of DMF and water. The reaction mixture was then heated at reflux overnight, allowed to cool to ambient temperature and concentrated under reduced pressure. Water was added to the residue and the solid was collected by filtration.
  • Step 2 cis-8-Methoxy-2-methyl-1,2,3,4,4a,5,6,10b-octahydro-1-oxo-3-phenylmethyl-benz[f]isoquinoline
  • reaction mixture was warmed to ⁇ 30° C and the solvent was evaporated with a stream of nitrogen gas.
  • TFA (12 mL) was added to the residue and the solution was cooled to 0°C
  • Sodium cyanoborohydride (1.12 g, 17.8 mmol) was added in two portions and the reaction mixture was allowed to warm to ambient temperature.
  • the reaction mixture was stirred at ambient temperature for 3 h and the TFA was evaporated by passing a stream of nitrogen through the reaction mixture overnight.
  • the residue was partitioned between methylene chloride and 1 N aqueous hydrochloric acid solution (4:1). The aqueous layer was extracted with two portions of methylene chloride.
  • Step 3 cis-8-Methoxy-2-methyl-1,2,3,4,4a,5,6,10b-octahydro-3-phenylmethyl-benz[f]isoquinoline hydrochloride
  • Step 3 1-Cyano-2-[1-(1,3-dioxolane)-3-phenylethyl]-6-methoxy-1,2,3,4-tetrahydronaphalene
  • p-Toluenesulfonic acid (5 g) was added and the reaction mixture was heated at reflux for 5 h, cooled to ambient temperature, and then partitioned between 1 N aqueous sodium hydroxide solution and diethyl ether (1:4) The aqueous layer was extracted with diethyl ether and the combined organic layers were washed with water, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure.
  • Step 4 1-Aminomethyl-2-[1-(1,3-dioxolane)-3-phenylethyl]-6-methoxy-1,2,3,4-tetrahydronaphalene
  • Step 5 cis and trans 1-(N-t-Butyloxycarbonylamino)methyl-2-[1-(1,3-dioxolane)-3-phenylethyl]-6-methoxy-1,2,3,4-tetrahydronaphalene
  • the combined organic layers were washed twice with water, once with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was chromatographed on silica gel eluted with hexane/diethyl ether (4:1 and 2:1) to give a total of 30.4 g (96% yield) of two products.
  • the first compound to elute from the column (73-5A) was the cis isomer: MS DCI-NH 3 M/Z: 468 (M + H) + ; MS DCI-NH 3 M/Z: 485 (M + NH 4 ) + .
  • the second compound to elute from the column (73-5B) was the trans isomer: MS DCl-NH 3 M/Z: 468 (M + H) + ; MS DCl-NH 3 M/Z: 485 (M+NH 4 ) + .
  • Step 6 cis-8-Methoxy-1,2,3,4,4a,5,6,10b-octahydro-3-phenylmethyl-benz[f]isoquinoline
  • the combined organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 5.5 g (98% yield) of the imine intermediate.
  • the imine was dissolved in 100 mL of methanol and sodium cyanoborohydride (3.5 g, 55 mmol) was added portionwise. Methanolic hydrogen chloride was added to maintain the pH of the reaction mixture at approximately 3. After the addition was complete, the reaction mixture was stirred at ambient temperature for 1 h and then acidified with methanolic hydrogen chloride to quench the excess sodium cyanoborohydride. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between 1 N aqueous sodium hydroxide and methylene chloride (1:4).
  • the aqueous layer was extracted with two portions of methylene chloride and the combined organic layers were dried over anhydrous magnesium sulfate, filtered and suspended on silica gel.
  • the product coated on silica gel was chromatographed on silica gel eluted with ethyl acetate/water/formic acid (19:0.5:0.5 followed by 18:1:1) to give the two diastereomeric title compounds in 90% total yield (5 g).
  • Step 7 1-(N-(+)-Menthylcarbonylamino)methyl-2-[1-(1,3-dioxolane)-3-phenylethyl]-6-methoxy-1,2,3,4-tetrahydronaphalene
  • the second compound to elute from the column was a mixture of the (3S, 4aR, 10aS) isomer and the (3R, 4aS, 10aR) isomer of the title compound.
  • the above reaction was repeated using (-) menthyl chloroformate to give the desired isomer as the first compound to elute from the column (73-7B) in 38% yield (0.62 g).
  • Step 8 (+) and (-) cis-8-Methoxy-2-methyl-1,2,3,4,4a,5,6,10b-octahydro-3-phenylmethyl-benz[f]isoquinoline hydrochloride
  • the reaction was quenched by the careful sequential addition of 250 ⁇ L of water, 250 ⁇ L of 4 N aqueous sodium hydroxide solution and 750 ⁇ L of water and stirred for 1 h at ambient temperature.
  • the suspension was filtered, the solid was washed with THF and the filtrate was concentrated in vacuo.
  • the residue was suspended in silica gel and chromatographed on silica gel eluted with ethyl acetate/water/formic acid (18:1:1).
  • the product was partitioned between 1 N aqueous sodium hydroxide and ethyl acetate (1:4) and the ethyl acetate solution was dried over anhydrous magnesium sulfate, filtered and concentrated to give the free amine of the title compound.
  • Step 1 trans/syn-8-Methoxy-2-methyl-1,2,3,4,4a,5,6,10b-octahydro-3-phenylmethyl-benz[f]isoquinoline
  • the combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered and suspended on silica gel.
  • the product adsorbed on silica gel was chromatographed on silica gel eluted with ethyl acetate/water/formic acid (28:1:1) to give 7.1 g of the intermediate trans imine as the first compound to elute from the column.
  • the imine was dissolved in 200 mL of methanol and sodium cyanoborohydride (4.4 g, 70 mmol) was added portionwise, maintaining the pH of the reaction mixture at approximately 3 using methanolic hydrogen chloride. After the addition was complete, the reaction mixture was stirred for 0.5 h and concentrated in vacuo.
  • Step 2 (-) trans8-Methoxy-2-methyl-1,2,3,4,4a,5,6,10b-octahydro-3-phenylmethyl-benz[f]isoquinoline hydrochloride
  • a-Tetralone (20 g, 137 mmol), commercially available from Aldrich Chemical Company, was combined with 200 mL of toluene, 30 mL of pyrrolidine and a catalytic amount of p-toluenesulfonic acid and the reaction mixture was heated at reflux for 4 days.
  • the reaction mixture was concentrated in vacuo and 300 mL of absolute ethyl alcohol and 25 mL of ethyl acrylate were added to the residue.
  • the reaction mixture was heated at reflux for 3 h and then 100 mL of water was added and reflux continued for 1 h.
  • Step 4 cis-2-Methyl-1,3,4,5,5a,6,7,11b-octahydro-3-oxo-2H-naphth[1,2-c]azepine
  • Step 5 cis-2-Methyl-1,3,4,5,5a,6,7,11b-octahydro-3-phenylmethyl-2H-naphth[1,2-c]azepine hydrochloride
  • Step 3 8-Methoxy-2-methyl-1,3,4,5,5a,6,7,11b-octahydro-3-oxo-2H-naphth[1,2-c]azepine
  • Step 4 8-Methoxy-2-methyl-1,3,4,5,5a,6,7,11b-octahydro-3-oxo-2H-naphth[1,2-c]azepine
  • Step 5 8-Methoxy-2-methyl-1,3,4,5,5a,6,7,11 b-octahydro-3-phenylmethyl-2H-naphth[1,2-c]azepine hydrochloride
  • the reaction was then quenched by the addition of saturated aqueous ammonium chloride and the aqueous mixture was extracted with methylene chloride. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was dissolved in methanol and 0.9 g of sodium cyanoborohydride was added portionwise. The pH of the reaction mixture was adjusted to 5 by the addition of methanol saturated with hydrogen chloride. After 10 min the pH was again adjusted to 5 by the addition of methanol saturated with hydrogen chloride. After 2 h at 0° C, methanol was added to quench the excess sodium cyanoborohydride.
  • Step 1 cis-2-Benzyl-1,3,4,5,5a,6,7,11b-octahydro-3-oxo-2H-naphth[1,2-c]azepine
  • Step 2 cis-2-Benzyl-1,3,4,5,5a,6,7,11 b-octahydro-3-phenylmethyl-2H-naphth[1,2-c]azepine hydrochloride
  • Step 3 cis-1,3,4,5,5a,6,7,11b-Octahydro-3-phenylmethyl-2H-naphth[1,2-c]azepine hydrochloride
  • Step 4 cis-2-((-)-Menthyloxycarbonyl)-1,3,4,5,5a,6,7,11b-octahydro-3-phenylmethyl-2H-naphth[1,2-c]azepine
  • Step 5 (+) cis-2-Methyl-1,3,4,5,5a,6,7,11b-octahydro-3-phenylmethyl-2H-naphth[1,2-c]azepine hydrochloride
  • Step 1 trans-2-Methyl-1,3,4,5,5a,6,7,11b-octahydro-3-oxo-2H-naphth[1,2-c]azepine
  • trans-2-methyl-1,3,4,5,5a,6,7,11b-octahydro-3-oxo-2H-naphth[1,2-c]azepine from Step 1 above, was converted to a total of 1.82 g (65% yield) of two isomeric products which were converted to their hydrochloride salts in diethyl ether saturated with hydrogen chloride.
  • the first compound to elute from the column (78A) was 988 mg of the trans/syn isomer, m.p. 213-215° C; MS DCI-NH 3 M/Z: 306 (M+H) + . Analysis calculated for C 22 H 28 CIN: C, 77.28; H, 8.25; N, 4.10. Found: C, 77.25; H, 8.19; N, 4.01.
  • reaction scheme I A By following the synthetic methods outlined in reaction scheme I A and reaction scheme I B, the following compounds (Example 80 - 105) can be prepared starting with 6-trifluoromethyl-a-tetralone or 7-trifluoromethyl-a-tetralone (B.R. Vogt, U.S. Patent Number 4,051,248, issued Sept. 27, 1977) and using the procedures described in the cited examples.
  • Examples 90 - 95 listed below are prepared in accordance with the procedures described in Examples 11, 12 and 13, .
  • Examples 102 - 105 listed below are prepared in accordance with the procedures described in Examples 17 and 18.

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WO1998030546A1 (fr) * 1997-01-08 1998-07-16 F. Hoffmann-La Roche Ag BENZO[e]ISOINDOLES ET BENZO[h]ISOQUINOLEINES TRICYCLIQUES
US6310208B1 (en) 1997-01-08 2001-10-30 Hoffmann-La Roche Inc. Serotonin receptor binding benzo[e]isoindoles and benzo[h]isoquinolines
WO2010103001A1 (fr) 2009-03-10 2010-09-16 N.V. Organon Dérivés hétérocycliques tricycliques
WO2010124005A1 (fr) 2009-04-21 2010-10-28 Purdue Research Foundation Modulateurs octahydrobenzoisoquinoléines de récepteurs de la dopamine, et utilisations de ces modulateurs

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JP3005287B2 (ja) * 1989-07-13 2000-01-31 ファルマシア・アンド・アップジョン・カンパニー （１，２ｎ）および（３，２ｎ）―炭素環式―２―アミノテトラリン誘導体
US6811773B1 (en) * 1993-12-22 2004-11-02 Human Genome Sciences, Inc. Human monocyte colony inhibitory factor (M-CIF) polypeptides
ES2304220B1 (es) * 2007-03-02 2009-09-11 Universidad De Zaragoza Composicion para el tratamiento de enfermedades infecciosas.
CN109803961B (zh) * 2016-09-23 2021-03-23 科研制药株式会社 (r)-5-(3,4-二氟苯基)-5-[(3-甲基-2-氧代吡啶-1(2h)-基)甲基]咪唑烷-2,4-二酮的制造方法及用于该制造的中间体

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WO1985003708A1 (fr) * 1984-02-17 1985-08-29 Arizona Board Of Regents Substance, composition de matiere et son procede d'utilisation
EP0201085A2 (fr) * 1985-05-07 1986-11-12 Pennwalt Corporation 6-Phényl-1,2,3,4,4a,5,6,10b-octahydrobenz(h)-isoquinoléines

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998030546A1 (fr) * 1997-01-08 1998-07-16 F. Hoffmann-La Roche Ag BENZO[e]ISOINDOLES ET BENZO[h]ISOQUINOLEINES TRICYCLIQUES
US6310208B1 (en) 1997-01-08 2001-10-30 Hoffmann-La Roche Inc. Serotonin receptor binding benzo[e]isoindoles and benzo[h]isoquinolines
CN1113872C (zh) * 1997-01-08 2003-07-09 弗·哈夫曼-拉罗切有限公司 三环苯并[e]异吲哚和苯并[h]异喹啉
WO2010103001A1 (fr) 2009-03-10 2010-09-16 N.V. Organon Dérivés hétérocycliques tricycliques
US8729274B2 (en) 2009-03-10 2014-05-20 Merck Sharp & Dohme B.V. Tricyclic heterocyclic derivatives
WO2010124005A1 (fr) 2009-04-21 2010-10-28 Purdue Research Foundation Modulateurs octahydrobenzoisoquinoléines de récepteurs de la dopamine, et utilisations de ces modulateurs
EP2421862A1 (fr) * 2009-04-21 2012-02-29 Purdue Research Foundation Modulateurs octahydrobenzoisoquinoléines de récepteurs de la dopamine, et utilisations de ces modulateurs
EP2421862A4 (fr) * 2009-04-21 2012-12-26 Purdue Research Foundation Modulateurs octahydrobenzoisoquinoléines de récepteurs de la dopamine, et utilisations de ces modulateurs
US9359303B2 (en) 2009-04-21 2016-06-07 Purdue Research Foundation Octahydrobenzoisoquinoline modulators of dopamine receptors and uses therefor

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